Canonical Allele Identifier: CA66957546

Gene: CHRND

Linked Data

• dbSNP Id: rs1018342449
• MyVariant Identifiers: chr2:g.233398821C>T (hg19) ; chr2:g.232534111C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534111C>T , CM000664.2:g.232534111C>T	GRCh38
NC_000002.11:g.233398821C>T , CM000664.1:g.233398821C>T	GRCh37
NC_000002.10:g.233107065C>T	NCBI36
NG_008028.1:g.12900C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1228C>T MANE Select	ENSP00000258385.3:p.Leu410=
ENST00000258385.7:c.1228C>T	ENSP00000258385.3:p.Leu410=
ENST00000441621.6:c.*410C>T	ENSP00000408819.2:n.*410C>T
ENST00000446616.1:c.*869C>T	ENSP00000410801.1:n.*869C>T
ENST00000543200.5:c.1183C>T	ENSP00000438380.1:p.Leu395=
NM_000751.2:c.1228C>T	NP_000742.1:p.Leu410=
NM_001256657.1:c.1183C>T	NP_001243586.1:p.Leu395=
NM_001311195.1:c.646C>T	NP_001298124.1:p.Leu216=
NM_001311196.1:c.925C>T	NP_001298125.1:p.Leu309=
NR_046333.1:c.-4294966323C>T
NR_046334.1:c.-4294966044C>T
XM_011510524.1:c.847C>T	XP_011508826.1:p.Leu283=
XM_011510524.2:c.847C>T	XP_011508826.1:p.Leu283=
NM_000751.3:c.1228C>T MANE Select	NP_000742.1:p.Leu410=
NM_001311195.2:c.646C>T	NP_001298124.1:p.Leu216=
NM_001311196.2:c.925C>T	NP_001298125.1:p.Leu309=
NM_001256657.2:c.1183C>T	NP_001243586.1:p.Leu395=